Evidence map›Paper›PMID 24854093›Full record

ArticleBiomaterials2014

The potential of label-free nonlinear optical molecular microscopy to non-invasively characterize the viability of engineered human tissue constructs.

Leng-Chun Chen, William R Lloyd, Shiuhyang Kuo, Hyungjin Myra Kim, Cynthia L Marcelo, Stephen E Feinberg, Mary-Ann Mycek

Abstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Leng-Chun ChenDepartment of Biomedical Engineering, University of Michigan College of Engineering & Medical School, 1101 Beal Avenue, Ann Arbor, MI 48109-2110, USA. Electronic address: lengleng@umich.edu.
William R LloydDepartment of Biomedical Engineering, University of Michigan College of Engineering & Medical School, 1101 Beal Avenue, Ann Arbor, MI 48109-2110, USA. Electronic address: billlloy@umich.edu.
Shiuhyang KuoDepartment of Oral and Maxillofacial Surgery, University of Michigan School of Dentistry, 1150 W. Medical Center Drive, Ann Arbor, MI 48109, USA. Electronic address: skuo@med.umich.edu.
Hyungjin Myra KimCenter for Statistical Consultation and Research, University of Michigan School of Public Health, 915 E. Washington, Ann Arbor, MI 48109-1070, USA. Electronic address: myrakim@umich.edu.
Cynthia L MarceloDepartment of Surgery, University of Michigan Medical School, 1150 W. Medical Center Drive, Ann Arbor, MI 48109, USA. Electronic address: cmarcelo@umich.edu.
Stephen E FeinbergDepartment of Oral and Maxillofacial Surgery, University of Michigan School of Dentistry, 1150 W. Medical Center Drive, Ann Arbor, MI 48109, USA; Department of Surgery, University of Michigan Medical School, 1150 W. Medical Center Drive, Ann Arbor, MI 48109, USA. Electronic address: sefein@med.umich.edu.
Mary-Ann MycekDepartment of Biomedical Engineering, University of Michigan College of Engineering & Medical School, 1101 Beal Avenue, Ann Arbor, MI 48109-2110, USA. Electronic address: mycek@umich.edu.

Funding

Non-invasive Assessment of Tissue Engineered Human Oral MucosaR01DE019431 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FEINBERG, STEPHEN ELLIOTT, MYCEK, MARY-ANN · 2009 to 2012
$3.0M
NIDCR NIH HHS R01 DE019431NIDCR NIH HHS R01-DE-019431
6 · The paper itself

Abstract

Nonlinear optical molecular imaging and quantitative analytic methods were developed to non-invasively assess the viability of tissue-engineered constructs manufactured from primary human cells. Label-free optical measures of local tissue structure and biochemistry characterized morphologic and functional differences between controls and stressed constructs. Rigorous statistical analysis accounted for variability between human patients. Fluorescence intensity-based spatial assessment and metabolic sensing differentiated controls from thermally-stressed and from metabolically-stressed constructs. Fluorescence lifetime-based sensing differentiated controls from thermally-stressed constructs. Unlike traditional histological (found to be generally reliable, but destructive) and biochemical (non-invasive, but found to be unreliable) tissue analyses, label-free optical assessments had the advantages of being both non-invasive and reliable. Thus, such optical measures could serve as reliable manufacturing release criteria for cell-based tissue-engineered constructs prior to human implantation, thereby addressing a critical regulatory need in regenerative medicine.

Indexed as

Tissue EngineeringCell DifferentiationCell SurvivalCross-Sectional StudiesHumansImage Processing, Computer-AssistedKeratinocytesMicroscopy, Fluorescence, MultiphotonMouth MucosaTissue ScaffoldsFluorescence lifetime imaging microscopy (FLIM)Label-free optical molecular imagingMultiphoton excitation microscopySecond-harmonic generation (SHG) imagingTissue engineeringTissue viability

Identifiers

PMID24854093
PMCPMC4106121

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.